Canonical Allele Identifier: CA517040899

Gene: AMER1

Linked Data

• MyVariant Identifiers: chrX:g.63411915G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.64192035G>T , CM000685.2:g.64192035G>T	GRCh38
NC_000023.10:g.63411915G>T , CM000685.1:g.63411915G>T	GRCh37
NC_000023.9:g.63328640G>T	NCBI36
NG_021345.1:g.18710C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000374869.8:c.1252C>A MANE Select	ENSP00000364003.4:p.Arg418=
ENST00000330258.3:c.1252C>A	ENSP00000329117.3:p.Arg418=
ENST00000374869.7:c.1252C>A	ENSP00000364003.3:p.Arg418=
NM_152424.3:c.1252C>A	NP_689637.3:p.Arg418=
XM_011530858.1:c.1252C>A	XP_011529160.1:p.Arg418=
NM_152424.4:c.1252C>A MANE Select	NP_689637.3:p.Arg418=